Canonical Allele Identifier: CA1139772927

Gene: LRP8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53247055C= , CM000663.2:g.53247055C=	GRCh38
NC_000001.10:g.53712727C= , CM000663.1:g.53712727C=	GRCh37
NC_000001.9:g.53485315C=	NCBI36
NG_011517.2:g.86095G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306052.12:c.2855G= MANE Select	ENSP00000303634.6:p.Arg952=
ENST00000347547.7:c.2345G=	ENSP00000334522.2:p.Arg782=
ENST00000465675.6:c.2489G=	ENSP00000437009.2:p.Arg830=
ENST00000480045.6:c.*1020G=	ENSP00000433554.2:n.*1020G=
ENST00000529670.6:c.393G=
ENST00000653217.1:c.2390G=	ENSP00000499777.1:p.Arg797=
ENST00000653810.1:c.1576G=
ENST00000654834.1:n.2315G=
ENST00000654947.1:c.357G=	ENSP00000499442.1:p.Ala119=
ENST00000656486.1:c.1985G=	ENSP00000499708.1:p.Arg662=
ENST00000657047.1:c.699G=
ENST00000657895.1:c.2336G=	ENSP00000499764.1:p.Arg779=
ENST00000658277.1:c.2090G=	ENSP00000499550.1:p.Arg697=
ENST00000658404.1:n.2183G=
ENST00000661457.1:c.*2074G=	ENSP00000499547.1:n.*2074G=
ENST00000662198.1:c.2468G=	ENSP00000499355.1:p.Arg823=
ENST00000662604.1:c.2162G=	ENSP00000499486.1:p.Arg721=
ENST00000662802.1:c.617G=
ENST00000667377.1:c.2677-1074G=	ENSP00000499405.1:n.2677-1074G=
ENST00000668071.1:c.2262G=
ENST00000668448.1:c.2630G=	ENSP00000499273.1:p.Arg877=
ENST00000668991.1:n.2568G=
ENST00000669432.1:n.9319G=
ENST00000306052.10:c.2855G=	ENSP00000303634.6:p.Arg952=
ENST00000347547.6:c.2345G=	ENSP00000334522.2:p.Arg782=
ENST00000354412.7:c.2066G=	ENSP00000346391.3:p.Arg689=
ENST00000371454.6:c.2678G=	ENSP00000360509.2:p.Arg893=
ENST00000465675.5:c.1337G=	ENSP00000437009.1:p.Arg446=
ENST00000480045.5:c.*1797G=	ENSP00000433554.1:n.*1797G=
ENST00000529670.5:c.328G=
ENST00000613948.4:c.2063G=	ENSP00000480025.1:p.Arg688=
NM_001018054.2:c.2678G=	NP_001018064.1:p.Arg893=
NM_004631.4:c.2855G=	NP_004622.2:p.Arg952=
NM_017522.4:c.2066G=	NP_059992.3:p.Arg689=
NM_033300.3:c.2345G=	NP_150643.2:p.Arg782=
XM_005271173.2:c.2894G=	XP_005271230.1:p.Arg965=
XM_005271174.2:c.2507G=	XP_005271231.1:p.Arg836=
XM_005271175.2:c.2468G=	XP_005271232.1:p.Arg823=
XM_006710881.2:c.2717G=	XP_006710944.1:p.Arg906=
XM_006710882.2:c.2669G=	XP_006710945.1:p.Arg890=
XM_011542094.1:c.2768G=	XP_011540396.1:p.Arg923=
XM_011542095.1:c.2378G=	XP_011540397.1:p.Arg793=
XM_011542097.1:c.2981G=	XP_011540399.1:p.Arg994=
XM_005271173.4:c.2894G=	XP_005271230.1:p.Arg965=
XM_005271174.3:c.2507G=	XP_005271231.1:p.Arg836=
XM_005271175.3:c.2468G=	XP_005271232.1:p.Arg823=
XM_006710881.4:c.2717G=	XP_006710944.1:p.Arg906=
XM_006710882.4:c.2669G=	XP_006710945.1:p.Arg890=
XM_011542094.2:c.2768G=	XP_011540396.1:p.Arg923=
XM_011542095.2:c.2378G=	XP_011540397.1:p.Arg793=
XM_017002265.1:c.2729G=	XP_016857754.1:p.Arg910=
XM_017002266.2:c.2492G=	XP_016857755.1:p.Arg831=
XM_017002267.1:c.1637G=	XP_016857756.1:p.Arg546=
XM_017002268.1:c.1637G=	XP_016857757.1:p.Arg546=
NM_001018054.3:c.2678G=	NP_001018064.1:p.Arg893=
NM_004631.5:c.2855G= MANE Select	NP_004622.2:p.Arg952=
NM_017522.5:c.2066G=	NP_059992.3:p.Arg689=
NM_033300.4:c.2345G=	NP_150643.2:p.Arg782=